March 1990
Volume 31, Issue 3
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Articles  |   March 1990
Herpes simplex virus glycoprotein D. Protective immunity against murine herpetic keratitis.
Author Affiliations
  • Y Inoue
    Department of Ophthalmology, Osaka University Medical School, Japan.
  • Y Ohashi
    Department of Ophthalmology, Osaka University Medical School, Japan.
  • Y Shimomura
    Department of Ophthalmology, Osaka University Medical School, Japan.
  • R Manabe
    Department of Ophthalmology, Osaka University Medical School, Japan.
  • M Yamada
    Department of Ophthalmology, Osaka University Medical School, Japan.
  • S Ueda
    Department of Ophthalmology, Osaka University Medical School, Japan.
  • S Kato
    Department of Ophthalmology, Osaka University Medical School, Japan.
Investigative Ophthalmology & Visual Science March 1990, Vol.31, 411-418. doi:
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    • Get Citation

      Y Inoue, Y Ohashi, Y Shimomura, R Manabe, M Yamada, S Ueda, S Kato; Herpes simplex virus glycoprotein D. Protective immunity against murine herpetic keratitis.. Invest. Ophthalmol. Vis. Sci. 1990;31(3):411-418.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

%$%%protective effect of glycoprotein D (gD) immunization against murine herpetic keratitis was investigated. gD was purified by affinity chromatography using anti-gD monoclonal antibodies. Prior immunization with gD was shown to be effective in protecting mice from both the development of stromal keratitis and the spread of the virus to the central nervous system. The level of serum antibodies for virus neutralization, as well as for complement-dependent cytolysis (CDC), was significantly elevated in gD-immunized animals. Cellular immunity, however, was not detected. These results indicate that two antibody-mediated defense mechanisms--virus neutralization and CDC--were responsible for the protective effect observed in our study.

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